Nerve Agents: from Discovery to Deterrence

Total Page:16

File Type:pdf, Size:1020Kb

Nerve Agents: from Discovery to Deterrence Books & arts reported. And the FDA, they say, has taken no action to correct misreporting of Study CIT-MD-18 in Forest’s application to license escitalopram to treat adolescent depression. Companies hand over raw trial data only if forced, usually in the course of litigation (which they budget for). Despite attempts to make the process more transparent, for example by mandating the preregistration of clinical trials, many of those data are not in the public domain. That’s why, the authors believe, these cases represent the tip of an iceberg. Falsifiable theory The authors agree that the randomized, placebo-controlled trial is the best method we have for testing drugs, and they argue that every scientific theory should be tested by, in Popper’s phrase, attempting to falsify the null hypothesis. In a trial, this means trying to disprove the idea that the treatment makes no difference. Adher- ing to this principle, researchers can never say for sure that a treatment is effective, but they can say definitively that it is not effective. However, the authors charge that drug companies have made even that impossible, by designing protocols that guarantee a pos- itive outcome or by spinning a negative one. One concern is the redefinition of endpoints mid-trial — a worry that resurfaced in the con- text of the US National Institute of Allergy and Infectious Diseases’ ongoing trial of the potential COVID-19 drug remdesivir, made by Gilead Sciences of Foster City, California. Partial solutions, such as requiring companies to deposit trial results in public databases, haven’t worked. The commercial disincentives are just too strong. Popper’s ideas have often been criticized. Theories are never truly falsified, critics say, just shown to be less wrong than others. But Soldiers involved in investigating the poisoning of Sergei and Yulia Skripal in Salisbury, UK, in 2018. we’ve gone too far down the road to relativism, counter Jureidini and McHenry; Popper offers a standard of integrity to which we must return. The only way to ensure that, they conclude, is to Nerve agents: from have trials conducted in a public-health system or by an independent institution funded by a tax on the industry. This would work only with discovery to deterrence government support, which has been lacking. Yet models do exist. The Mario Negri Institute for Pharmacological Research in Milan, Italy, Chemical weapons treaties are not enough — scientists has been conducting independent clinical trials for nearly 60 years. and industry play a part, too. By Leiv K. Sydnes The current pandemic might provide the perfect opportunity to acknowledge that there is a problem: ill people need treatments hen the Russian former military Enter Toxic, a round-up of the invention, and the well need a vaccine. Quoting ancient officer Sergei Skripal and his production, proliferation and use of nerve Greek historian Thucydides, the authors write: daughter Yulia were poisoned agents. Author Dan Kaszeta has spent a “There will be justice … when those who are with a ‘novichok’ nerve agent in career in defence and security, specializing in not injured are as outraged as those who are.” the tranquil UK city of Salisbury chemical, biological, radiological and nuclear Win March 2018, it led to widespread fear that materials. He worked for the US military, gov- Laura Spinney is a science writer based in Paris. similar mysterious chemicals, illegal under ernment and secret service before moving to Her most recent book is Pale Rider: The Spanish international conventions, might be deployed the United Kingdom and becoming a security Flu of 1918 and How it Changed the World. elsewhere. What were they, where did they consultant. Drawing on this experience and an e-mail: [email protected] come from and what made them so deadly? array of authoritative documents, he follows COX/GETTY RUFUS 28 | Nature | Vol 583 | 2 July 2020 ©2020 Spri nger Nature Li mited. All rights reserved. ©2020 Spri nger Nature Li mited. All rights reserved. make insecticides to secure Germany’s food shameful history. The invasion by the United supply, led by Gerhard Schrader at chem- States and its allies in March 2003 had the ical and pharmaceuticals giant IG Farben declared aim of eliminating weapons of mass in Leverkusen from 1934. The research pro- destruction, in particular chemical weapons. duced a liquid compound, eventually called None was found. In February that year, US tabun, with a toxicity far beyond anything seen secretary of state Colin Powell had presented before (0.1 milligrams of tabun per kilogram ‘evidence’ for the presence of such weapons in of body weight killed the monkeys used for Iraq before the United Nations security coun- testing). Almost at once, the Nazi authorities cil; this is now generally accepted to have been launched a massive programme, involving uni- based on faulty intelligence. versity scientists, the chemical industry and Kaszeta devotes just half a page to this con- military personnel, to develop weapons that flict. He does not mention false or fabricated would distribute nerve agents — first tabun and intelligence, and describes as “conventional later sarin — in a predictable manner in com- wisdom” the statement that the invading bat, without harming those who applied them. forces did not discover any chemical weap- ons, leaving the impression that the weapons “Manufacturers of the key might indeed have existed. He seems to imply that Hussein’s previous use of nerve agents ingredient refused to supply justified his punishment. This was not an argu- goods for use in weapons ment used by world leaders as they discussed production.” an invasion. To me, the sacrifice of truth in the process of this discussion seemed shattering. Toxic is at its best when the people making This happened even though chemical decisions, taking initiatives and violating weapons were not part of German military agreements appear as characters in the strategy. Two factors were decisive. First was a chronological narrative, from the beginning capable industrial partner: IG Farben was avail- to about 1950. At that point, Soviet and able and willing. Second, the German leader- Western powers had acquired enough knowl- ship believed that the United States had nerve edge about nerve-agent production, through agents and could retaliate if attacked. I don’t interrogation of German chemists and inves- think these two factors are as independent as tigations of actual chemical weapons, to start they seem. People such as IG Farben executive large-scale production themselves. Otto Ambros, who kept Adolf Hitler informed Later sections are bogged down in detail. about perceived US weapons capabilities, were Yes, it is very difficult to turn tonnes of nerve also central in running the industrial produc- agents into safe and effective weapons, but tion of the nerve agents, so had a personal we don’t need elaborate descriptions of artil- business interest. Ambros made a fortune, lery-shell testing to demonstrate the point. even though the Nazi military did not, in the More important, bombs aren’t necessary to event, deploy the weapons. cause panic and death. It was relatively easy for the Aum Shinrikyo cult to make and use Soldiers involved in investigating the poisoning of Sergei and Yulia Skripal in Salisbury, UK, in 2018. Ethical standards sarin in Tokyo in 1995. Likewise, a skilled per- What would have happened had the German son with the right chemicals could prepare and the development of these deadly compounds, chemical industry declined to become apply novichoks. The 1997 Chemical Weapons from the first discoveries in Germany in the involved? Kaszeta does not discuss this, but Convention and its implementing body, the 1930s to the Salisbury attack. He shows how perhaps nerve-agent weapons would not have Organisation for the Prohibition of Chemical fear of nerve agents influenced world events, been developed. That was the case for the dec- Weapons, cannot prevent this. such as the invasion of Iraq in 2003. And he ades-long US programme to develop ‘binary’ Kaszeta’s book is informative; it should reminds us that even with an international chemical weapons, which contain precursor satisfy curious non-specialists able to digest convention banning them, the threat of chem- compounds that are mixed to produce the details. The omission of chemical structures is ical weapons being used outside conventional toxic agent on detonation. This programme generally no drawback, but when compounds warfare is ever-present. Stronger on the early was terminated around 1990, after Mobay are described as similar, some drawings in an history than on more recent politics, Toxic is and Occidental, the two domestic manufac- appendix would have clarified the point. Yet a useful introduction to the subject. turers of the key ingredient thionyl chloride, the take-home message is clear: nerve agents The first nerve agents were the unintended refused to supply it because company policy are fairly easy to make, but difficult to turn into consequence of a civil research project to forbade the sale of goods for use in weapons weapons. Their application in small quantities production. by aggressive individuals therefore remains Toxic: A History Unfortunately, the absence of such an ethical a threat. of Nerve Agents, standard enabled Iraqi president Saddam From Nazi Germany Hussein to start large-scale production of Leiv Sydnes is a professor of organic to Putin’s Russia tabun and sarin in 1981, using equipment chemistry at the University of Bergen in Dan Kaszeta Hurst (2020) and chemicals supplied by European and US Norway. He chaired the international task companies. group that assessed the impact of scientific After the first Gulf War (1990–91), Iraq’s advances on the Chemical Weapons chemical weapons were destroyed, making Convention in 2007 and 2012.
Recommended publications
  • ASM 2013 Countermotions.Pdf
    Christiane Schnura, Schweidnitzer Str. 41, 40231 Düsseldorf Christiane Schnura, Schweidnitzer Str. 41, 40231 Düsseldorf Bayer Aktiengesellschaft Gebäude Q 26 (Rechtsabteilung) Kaiser-Wilhelm-Allee 51368 Leverkusen Annual Stockholders’ Meeting on April 26, 2013 I hereby notify you that I will oppose the proposals of the Board of Management and the Supervisory Board as regards Items 2 and 3 of the Agenda, and will induce the other stockholders to vote in favor of the following countermotions. Countermotion to Item 2: The actions of the members of the Board of Management are not ratified The BAYER Group is responsible for many environmental and social problems. The Board of Management bears responsibility for this, and for this reason its actions should not be ratified. The following is a selection of current problem areas. Labeling of genetically engineered products BAYER contributed USD 2 million to a campaign operated by chemical corporations in the United States which resulted in an initiative to have genetically engineered food products labeled accordingly being defeated. Proposition 37, an initiative put forward in the federal state of California which called for mandatory European-style labeling, went to the ballot on Presidential Election Day, November 6. The companies invested more than USD 40 million in their advertising campaign, roughly ten times more than the proponents of the initiative. This is a classic example of double standards. In Europe it goes without saying that genetically modified ingredients are declared on the labeling of a food product. In the United States, on the other hand, spurious arguments are put forward to prevent labeling of this kind.
    [Show full text]
  • Historical Perspectives on Apple Production: Fruit Tree Pest Management, Regulation and New Insecticidal Chemistries
    Historical Perspectives on Apple Production: Fruit Tree Pest Management, Regulation and New Insecticidal Chemistries. Peter Jentsch Extension Associate Department of Entomology Cornell University's Hudson Valley Lab 3357 Rt. 9W; PO box 727 Highland, NY 12528 email: [email protected] Phone 845-691-7151 Mobile: 845-417-7465 http://www.nysaes.cornell.edu/ent/faculty/jentsch/ 2 Historical Perspectives on Fruit Production: Fruit Tree Pest Management, Regulation and New Chemistries. by Peter Jentsch I. Historical Use of Pesticides in Apple Production Overview of Apple Production and Pest Management Prior to 1940 Synthetic Pesticide Development and Use II. Influences Changing the Pest Management Profile in Apple Production Chemical Residues in Early Insect Management Historical Chemical Regulation Recent Regulation Developments Changing Pest Management Food Quality Protection Act of 1996 The Science Behind The Methodology Pesticide Revisions – Requirements For New Registrations III. Resistance of Insect Pests to Insecticides Resistance Pest Management Strategies IV. Reduced Risk Chemistries: New Modes of Action and the Insecticide Treadmill Fermentation Microbial Products Bt’s, Abamectins, Spinosads Juvenile Hormone Analogs Formamidines, Juvenile Hormone Analogs And Mimics Insect Growth Regulators Azadirachtin, Thiadiazine Neonicotinyls Major Reduced Risk Materials: Carboxamides, Carboxylic Acid Esters, Granulosis Viruses, Diphenyloxazolines, Insecticidal Soaps, Benzoyl Urea Growth Regulators, Tetronic Acids, Oxadiazenes , Particle Films, Phenoxypyrazoles, Pyridazinones, Spinosads, Tetrazines , Organotins, Quinolines. 3 I Historical Use of Pesticides in Apple Production Overview of Apple Production and Pest Management Prior to 1940 The apple has a rather ominous origin. Its inception is framed in the biblical text regarding the genesis of mankind. The backdrop appears to be the turbulent setting of what many scholars believe to be present day Iraq.
    [Show full text]
  • Nerve Agent - Lntellipedia Page 1 Of9 Doc ID : 6637155 (U) Nerve Agent
    This document is made available through the declassification efforts and research of John Greenewald, Jr., creator of: The Black Vault The Black Vault is the largest online Freedom of Information Act (FOIA) document clearinghouse in the world. The research efforts here are responsible for the declassification of MILLIONS of pages released by the U.S. Government & Military. Discover the Truth at: http://www.theblackvault.com Nerve Agent - lntellipedia Page 1 of9 Doc ID : 6637155 (U) Nerve Agent UNCLASSIFIED From lntellipedia Nerve Agents (also known as nerve gases, though these chemicals are liquid at room temperature) are a class of phosphorus-containing organic chemicals (organophosphates) that disrupt the mechanism by which nerves transfer messages to organs. The disruption is caused by blocking acetylcholinesterase, an enzyme that normally relaxes the activity of acetylcholine, a neurotransmitter. ...--------- --- -·---- - --- -·-- --- --- Contents • 1 Overview • 2 Biological Effects • 2.1 Mechanism of Action • 2.2 Antidotes • 3 Classes • 3.1 G-Series • 3.2 V-Series • 3.3 Novichok Agents • 3.4 Insecticides • 4 History • 4.1 The Discovery ofNerve Agents • 4.2 The Nazi Mass Production ofTabun • 4.3 Nerve Agents in Nazi Germany • 4.4 The Secret Gets Out • 4.5 Since World War II • 4.6 Ocean Disposal of Chemical Weapons • 5 Popular Culture • 6 References and External Links --------------- ----·-- - Overview As chemical weapons, they are classified as weapons of mass destruction by the United Nations according to UN Resolution 687, and their production and stockpiling was outlawed by the Chemical Weapons Convention of 1993; the Chemical Weapons Convention officially took effect on April 291997. Poisoning by a nerve agent leads to contraction of pupils, profuse salivation, convulsions, involuntary urination and defecation, and eventual death by asphyxiation as control is lost over respiratory muscles.
    [Show full text]
  • Warning: the Following Lecture Contains Graphic Images
    What the новичок (Novichok)? Why Chemical Warfare Agents Are More Relevant Than Ever Matt Sztajnkrycer, MD PHD Professor of Emergency Medicine, Mayo Clinic Medical Toxicologist, Minnesota Poison Control System Medical Director, RFD Chemical Assessment Team @NoobieMatt #ITLS2018 Disclosures In accordance with the Accreditation Council for Continuing Medical Education (ACCME) Standards, the American Nurses Credentialing Center’s Commission (ANCC) and the Commission on Accreditation for Pre-Hospital Continuing Education (CAPCE), states presenters must disclose the existence of significant financial interests in or relationships with manufacturers or commercial products that may have a direct interest in the subject matter of the presentation, and relationships with the commercial supporter of this CME activity. The presenter does not consider that it will influence their presentation. Dr. Sztajnkrycer does not have a significant financial relationship to report. Dr. Sztajnkrycer is on the Editorial Board of International Trauma Life Support. Specific CW Agents Classes of Chemical Agents: The Big 5 The “A” List Pulmonary Agents Phosgene Oxime, Chlorine Vesicants Mustard, Phosgene Blood Agents CN Nerve Agents G, V, Novel, T Incapacitating Agents Thinking Outside the Box - An Abbreviated List Ammonia Fluorine Chlorine Acrylonitrile Hydrogen Sulfide Phosphine Methyl Isocyanate Dibotane Hydrogen Selenide Allyl Alcohol Sulfur Dioxide TDI Acrolein Nitric Acid Arsine Hydrazine Compound 1080/1081 Nitrogen Dioxide Tetramine (TETS) Ethylene Oxide Chlorine Leaks Phosphine Chlorine Common Toxic Industrial Chemical (“TIC”). Why use it in war/terror? Chlorine Density of 3.21 g/L. Heavier than air (1.28 g/L) sinks. Concentrates in low-lying areas. Like basements and underground bunkers. Reacts with water: Hypochlorous acid (HClO) Hydrochloric acid (HCl).
    [Show full text]
  • SARIN the History and Politics of a Chemical Warfare Agent
    SARIN The History and Politics of a Chemical Warfare Agent Sarin: A Nerve Agent Sarin, a.k.a. GB, and its other organophosphorus relatives (VX, etc.) are members of the class of chemical weapons known as "nerve agents." These SARIN compounds target the central nervous system where they serve as cholinesterase inhibitors, blocking nerve impulse transmission across synapses. This effect can be lethal. From Sarin's MSDS: "Symptoms of overexposure may occur within minutes or hours, depending upon dose. They include: miosis (constriction of pupils) and visual effects, (C4H10FO2P) headaches and pressure sensation, runny nose and nasal congestion, salivation, Isopropylmethanefluorophosphonate tightness in the chest, nausea, vomiting, giddiness, anxiety, difficulty in thinking and sleeping, nightmares, muscle twitches, tremors, weakness, Common Names: GB, Zarin abdominal cramps, diarrhea, involuntary urination and defecation. With severe A volatile, colorless, odorless liquid exposure symptoms progress to convulsions and respiratory failure." Least-Effect Dose: Japan subway: Vomiting of blood 0.002 mg/L over 15 inhalations For detoxification: Lethal Dose: 0.07 mg/L over 15 inhalations Treat contaminated area with 10% NaOH solution or In humans: "administer, in rapid succession, all three Nerve Agent 1.7 g on skin (for a 70 kg human) Antidote Kit(s), Mark I injectors (or atropine if directed by physician). " The History of Nerve Agents 1936 Dr. Gerhard Schrader, a chemist at IG Farben, discovered the first of the organophosphorus nerve agents, Tabun, en route to finding more effective pesticides. The project had started in 1934. 1942-45 Germans develop the first generation "G" nerve agents. Schrader and colleagues make 2000 new compounds.
    [Show full text]
  • 6/26/2012 1 Malathion Impurities Dr. Yehia Ibrahim
    1 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 2 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 3 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 Organophosphates and Germany • 1820s: investigations into organophosphate (OP) chemistry began • Early 1900s: several OP compounds synthesized • 1930s: toxicity of OPs becoming recognized • 1940s: insecticidal action observed by Germany during WWII 4 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 Organophosphates and Germany • Group led by Gerhard Schrader searching for substitutes to nicotine as an insecticide – Nicotine in short supply during WWII – Developed a number of incredibly toxic nerve agents Sarin Soman Tabun 5 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 Organophosphates and Germany • Schrader’s group also created some of the first commercial OP insecticides Dimefox TEPP Schradan Parathion 6 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 After WWII • Schrader’s research records were captured by Allied forces – Led to massive increase in interest in OP insecticides • Early OPs – very effective against insects – Much more toxic to vertebrates than organochlorine insecticides – Nonpersistent and chemically unstable 7 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 Malathion • First produced by American Cyanamid in 1950 • Very safe due to its low vertebrate toxicity • Used on most fruits, vegetables and forage crops • Works on a wide range of insect pests 8 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 9 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 Diethyl 2-[(dimethoxyphosphorothioyl)sulfanyl]butanedioate 10 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 11 Malathion Impurities Dr. Yehia Ibrahim 6/26/2012 O Diethyl Maleate C CH O CH CH 2 3 S + CH O CH CH 2 3 CH O P O CH C O 3 3 S C S O CH CH O CH CH O P S 2 3 H O 3 O CH O CH C 2 2 CH + CH C 3 CH O CH 2 CH 3 Malathion 3 O CH 3 CH 2 O CH C O Diethyl Fumarate 12 Malathion Impurities Dr.
    [Show full text]
  • View Is Primarily on Addressing the Issues of Non-Permanently Charged Reactivators and the Development of Treatments for Aged Ache
    Design, Synthesis, and Evaluation of Therapeutics for the Treatment of Organophosphorus Poisoning by Nerve Agents and Pesticides Dissertation Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Andrew Joseph Franjesevic Graduate Program in Chemistry The Ohio State University 2019 Dissertation Committee Professor Christopher M. Hadad, Advisor Professor Thomas J. Magliery Professor David Nagib Professor Jonathan R. Parquette Copyrighted by Andrew Joseph Franjesevic 2019 2 Abstract Organophosphorus (OP) compounds, both pesticides and nerve agents, are some of the most lethal compounds known to man. Although highly regulated for both military and agricultural use in Western societies, these compounds have been implicated in hundreds of thousands of deaths annually, whether by accidental or intentional exposure through agricultural or terrorist uses. OP compounds inhibit the function of the enzyme acetylcholinesterase (AChE), and AChE is responsible for the hydrolysis of the neurotransmitter acetylcholine (ACh), and it is extremely well evolved for the task. Inhibition of AChE rapidly leads to accumulation of ACh in the synaptic junctions, resulting in a cholinergic crisis which, without intervention, leads to death. Approximately 70-80 years of research in the development, treatment, and understanding of OP compounds has resulted in only a handful of effective (and approved) therapeutics for the treatment of OP exposure. The search for more effective therapeutics is limited by at least three major problems: (1) there are no broad scope reactivators of OP-inhibited AChE; (2) current therapeutics are permanently positively charged and cannot cross the blood-brain barrier efficiently; and (3) current therapeutics are ineffective at treating the aged, or dealkylated, form of AChE that forms following inhibition of of AChE by various OPs.
    [Show full text]
  • NIH Public Access Provided by CDC Stacks Author Manuscript Chem Biol Interact
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE NIH Public Access provided by CDC Stacks Author Manuscript Chem Biol Interact. Author manuscript; available in PMC 2014 July 23. NIH-PA Author ManuscriptPublished NIH-PA Author Manuscript in final edited NIH-PA Author Manuscript form as: Chem Biol Interact. 2013 March 25; 203(1): 85–90. doi:10.1016/j.cbi.2012.10.019. Proteomic analysis of adducted butyrylcholinesterase for biomonitoring organophosphorus exposures Judit Marsillacha,b, Edward J. Hsiehb, Rebecca J. Richtera,b, Michael J. MacCossb, and Clement E. Furlonga,b,* Judit Marsillach: [email protected]; Edward J. Hsieh: [email protected]; Rebecca J. Richter: [email protected]; Michael J. MacCoss: [email protected]; Clement E. Furlong: [email protected] aDept. of Medicine (Division of Medical Genetics), University of Washington, 98195 Seattle, WA, USA bDept. of Genome Sciences, University of Washington, 98195 Seattle, WA, USA Abstract Organophosphorus (OP) compounds include a broad group of toxic chemicals such as insecticides, chemical warfare agents and antiwear agents. The liver cytochromes P450 bioactivate many OPs to potent inhibitors of serine hydrolases. Cholinesterases were the first OP targets discovered and are the most studied. They are used to monitor human exposures to OP compounds. However, the assay that is currently used has limitations. The mechanism of action of OP compounds is the inhibition of serine hydrolases by covalently modifying their active-site serine. After structural rearrangement, the complex OP inhibitor-enzyme is irreversible and will remain in circulation until the modified enzyme is degraded. Mass spectrometry is a sensitive technology for analyzing protein modifications, such as OP-adducted enzymes.
    [Show full text]
  • Pharmacists Adolf Schall and Ernst Ratzlaff and the Synthesis of Tabun-Like Compounds: a Brief History
    ORIGINAL ARTICLES Herbert Wertheim College of Medicine, Florida International University, Miami, FL, USA Pharmacists Adolf Schall and Ernst Ratzlaff and the synthesis of tabun-like compounds: a brief history G. A. Petroianu Received February 12, 2014, accepted March 25, 2014 Prof. Dr. med. Georg A Petroianu, Herbert Wertheim College of Medicine, Florida International University, Depart- ment of Cellular Biology & Pharmacology, University Park (11200 SW 8th Street), Miami, 33199 FL georg.petroianu@fiu.edu Pharmazie 69: 780–784 (2014) doi: 10.1691/ph.2014.4028 The history of the synthesis of organophosphate inhibitors of cholinesterase starting with the synthe- sis of tetraethyl-pyrophosphate by Moschnin(e) and de Clermont and leading to the recognition about half a century later of the toxicity of the phosphor ester by Lange and von Krueger has been told in great detail previously. An almost parallel history –described originally by Bo Holmstedt – exists for organophosphonate inhibitors of cholinesterase starting with the synthesis (1898) in Rostock of diethylamido-ethoxy-phosphoryl-cyanide by the pharmacist Adolph Schall (1870–1957), a graduate stu- dent of August Michaelis (1847–1916), the re-examination of the chemical structure of the Schall compound (1903) by Michaelis, recognition (1937) of the toxicity of class by Gerhard Schrader (1903–1990) and con- firmation (1951) of the structure by Bo Holmstedt (1919–2002). This short report attempts to shed some light on the life of the pharmacists and chemists involved in the synthesis of the first P-CN organophos- phonate inhibitor of cholinesterase, focusing on the two less known pharmacists, the graduate students of Professor Michaelis Adolph Schall and Ernst Ratzlaff (1870–1948).
    [Show full text]
  • The Therapeutic Efficacy of Oxime Treatment in Cyclosarin- Poisoned Mice Pretreated with a Combination of Pyridostigmine Benactyzine and Trihexyphenidyl
    Journal of Applied Biomedicine 2: 163–167, 2004 ISSN 1214–0287 ORIGINAL ARTICLE The therapeutic efficacy of oxime treatment in cyclosarin- poisoned mice pretreated with a combination of pyridostigmine benactyzine and trihexyphenidyl Lucie Ševelová, Kamil Kuča, Gabriela Krejčová, Josef Vachek Purkyně Military Medical Academy, Department of Toxicology, Hradec Králové, Czech Republic Received 30th January 2004. Revised 20th March 2004. Published online 25th April 2004. Summary The present study was performed to assess and compare the therapeutic efficacy of various oximes (methoxime, BI-6, HI-6) combined with benactyzine (BNZ) in cyclosarin (GF-agent)- poisoned mice and to evaluate the influence of pretreatment with PANPAL (pyridostigmine, benactyzine and trihexyphenidyl) on the effect of antidotal treatment in mice poisoned with the GF-agent. In the first part of our experiment, methoxime, BI-6 or HI-6 in combination with benactyzine were used for the treatment of GF-poisoned mice. In the second part of the experiment the animals were pretreated with PANPAL 60 min before the GF-agent challenge and then the oxime therapy was applied in the same time scheme as before. All the therapeutic regimens showed a protective ratio higher than 2 and significantly increased the LD50 of GF-agent. The most efficacious oxime in decreasing of GF-agent toxicity was HI-6. PANPAL increased the protective ratios of all therapeutic regimens in comparison with administration of the oxime and BNZ alone. From the results obtained, the combination of pretreatment with PANPAL and following therapy with BNZ and HI-6 seems to be the most efficacious therapeutic regimen for treatment of GF-agent-poisoned mice.
    [Show full text]
  • The Toxicity of Parathion to Orconectes Rusticus and Viviparus Malleatus
    University of Rhode Island DigitalCommons@URI Open Access Dissertations 1978 THE TOXICITY OF PARATHION TO ORCONECTES RUSTICUS AND VIVIPARUS MALLEATUS Leslie Alan Goldsmith University of Rhode Island Follow this and additional works at: https://digitalcommons.uri.edu/oa_diss Recommended Citation Goldsmith, Leslie Alan, "THE TOXICITY OF PARATHION TO ORCONECTES RUSTICUS AND VIVIPARUS MALLEATUS" (1978). Open Access Dissertations. Paper 151. https://digitalcommons.uri.edu/oa_diss/151 This Dissertation is brought to you for free and open access by DigitalCommons@URI. It has been accepted for inclusion in Open Access Dissertations by an authorized administrator of DigitalCommons@URI. For more information, please contact [email protected]. THE TOXICITY OF PARATHION TO ORCONECTES RUSTICUS AND VIVIPARUS MALLEATUS BY LESLIE ALAN GOLDSMITH A DISSERTATION SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY IN PHARMACEUTICAL SCIENCES (PHARMACOLOGY AND TOXICOLOGY) UNIVERSITY OF RHODE ISLAND 1978 DOCTOR OF PHILOSOPHY DISSERTATION OF LESLIE ALAN GOLDSMITH Approved: Dissertation Committee Dean of the Graduate School UNIVERSITY OF RHODE ISLAND 1978 PARATHION TOXICITY TO ORCONECTES & VIVIPARUS Abstract Parathion is an organophosphate pesticide used in great quantities in the United States and around the world. The mechanism of toxicity for parathion in mammals has been attributed to its enzymatic desulfuration to its oxygen analog paraoxon which subsequently fonns a covalent bond with acetylcholinesterase
    [Show full text]
  • Comparative Activation of Organophosphorus Insecticides by Liver Microsomes Richard Emanuel Johnsen Iowa State University
    Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1962 Comparative activation of organophosphorus insecticides by liver microsomes Richard Emanuel Johnsen Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Zoology Commons Recommended Citation Johnsen, Richard Emanuel, "Comparative activation of organophosphorus insecticides by liver microsomes " (1962). Retrospective Theses and Dissertations. 2004. https://lib.dr.iastate.edu/rtd/2004 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. This dissertation has been 62—3010 microfilmed exactly as received JOHNSEN, Richard Emanuel, 1936- COMPARATIVE ACTIVATION OF ORGANO­ PHOSPHOROUS INSECTICIDES BY LIVER MICROSOMES. Iowa State University of Science and Technology Ph.D., 1962 Zoology University Microfilms, Inc., Ann Arbor, Michigan COMPARATIVE ACTIVATION OF ORGANOPHOSPHORUS INSECTICIDES BY LIVER MICROSOMES bY Richard Emanuel Johnsen A Dissertation Submitted to the Graduate Faculty in Partial Fulfillment of The Requirements for the Degree of DOCTOR OF PHILOSOPHY Major Subject: Entomology Approved: Signature was redacted for privacy. In Charge of Major Work Signature was redacted
    [Show full text]